A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400639



Internal ID21058192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20175525..20195031hg38UCSC Ensembl
chr6:20175756..20195262hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3819507
hg1919507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236820
Samples
Known GenesMBOAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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